Variant report

Variant	esv3356756
Chromosome Location	chr19:45147137-45149985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:357)
CpG islands
(count:183)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr19:45146888-45147518	A549	lung:	n/a	n/a
2	ATF3	chr19:45146708-45147481	A549	lung:	n/a	n/a
3	BCL3	chr19:45146679-45148185	A549	lung:	n/a	chr19:45147570-45147583 chr19:45147200-45147209 chr19:45147572-45147581 chr19:45147569-45147582
4	BCL3	chr19:45146754-45147958	A549	lung:	n/a	chr19:45147570-45147583 chr19:45147200-45147209 chr19:45147572-45147581 chr19:45147569-45147582
5	BRCA1	chr19:45147697-45147861	H1-hESC	embryonic stem cell:	n/a	n/a
6	CCNT2	chr19:45147015-45147392	K562	blood:	n/a	n/a
7	CEBPB	chr19:45146505-45147395	A549	lung:	n/a	n/a
8	CEBPD	chr19:45146879-45147437	HepG2	liver:	n/a	n/a
9	CHD1	chr19:45147276-45147322	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD1	chr19:45148016-45148023	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD1	chr19:45146500-45148251	IMR90	lung:	n/a	n/a
12	CREB1	chr19:45147522-45148029	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr19:45146652-45148107	HepG2	liver:	n/a	n/a
14	CREB1	chr19:45147641-45147904	A549	lung:	n/a	n/a
15	CREB1	chr19:45146771-45148000	A549	lung:	n/a	n/a
16	CTBP2	chr19:45146913-45147958	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr19:45147340-45147490	HRE	kidney:	n/a	n/a
18	CTCF	chr19:45147393-45147452	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr19:45147330-45147536	MCF-7	breast:	n/a	n/a
20	CTCF	chr19:45147381-45147464	MCF-7	breast:	n/a	n/a
21	CTCF	chr19:45147360-45147510	HCM	heart:	n/a	n/a
22	CTCF	chr19:45147020-45147170	AG04449	skin:	n/a	n/a
23	CTCF	chr19:45147384-45147500	Gliobla	brain:	n/a	n/a
24	CTCF	chr19:45147320-45147470	AG04449	skin:	n/a	n/a
25	CTCF	chr19:45147843-45147965	MCF-7	breast:	n/a	n/a
26	CTCF	chr19:45147400-45147550	HMEC	breast:	n/a	n/a
27	CTCF	chr19:45147360-45147510	HEK293	kidney:	n/a	n/a
28	CTCF	chr19:45147340-45147490	AG09319	gingival:	n/a	n/a
29	CTCF	chr19:45147400-45147550	HepG2	liver:	n/a	n/a
30	CTCF	chr19:45147340-45147490	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr19:45147404-45147458	HepG2	liver:	n/a	n/a
32	CTCF	chr19:45147300-45147450	AG04449	skin:	n/a	n/a
33	CTCF	chr19:45147300-45147450	Caco-2	colon:	n/a	n/a
34	CTCF	chr19:45147340-45147490	BJ	skin:	n/a	n/a
35	CTCF	chr19:45147320-45147470	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr19:45147400-45147550	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr19:45147817-45147911	MCF-7	breast:	n/a	n/a
38	CTCF	chr19:45147320-45147470	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr19:45147340-45147490	RPTEC	kidney:	n/a	n/a
40	CTCF	chr19:45146870-45147405	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr19:45147260-45147410	HepG2	liver:	n/a	n/a
42	CTCF	chr19:45147340-45147490	NHEK	skin:	n/a	n/a
43	CTCF	chr19:45147400-45147471	Fibrobl	skin:	n/a	n/a
44	CTCF	chr19:45147300-45147450	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr19:45147345-45147521	MCF-7	breast:	n/a	n/a
46	CTCF	chr19:45147560-45147710	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr19:45147320-45147470	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr19:45147340-45147490	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr19:45147380-45147530	GM06990	blood:	n/a	n/a
50	CTCF	chr19:45147354-45147487	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:45147715-45147765	A549	lung:	n/a
2	chr19:45147316-45147366	NHBE	bronchial:	n/a
3	chr19:45147715-45147765	HPAEpiC	pulmonary alveolar:	n/a
4	chr19:45147440-45147490	NHBE	bronchial:	n/a
5	chr19:45147715-45147765	HCF	heart:	n/a
6	chr19:45147715-45147765	U87	brain:	n/a
7	chr19:45147440-45147490	GM12892	blood:	n/a
8	chr19:45147316-45147366	HMEC	breast:	n/a
9	chr19:45147440-45147490	ProgFib	skin:	n/a
10	chr19:45147715-45147765	HIPEpiC	eye:	n/a
11	chr19:45147715-45147765	Caco-2	colon:	n/a
12	chr19:45147715-45147765	AG10803	skin:	n/a
13	chr19:45147715-45147765	Hela-S3	cervix:	n/a
14	chr19:45147316-45147366	GM12892	blood:	n/a
15	chr19:45147316-45147366	HL-60	blood:	n/a
16	chr19:45147715-45147765	SK-N-SH	brain:	n/a
17	chr19:45147316-45147366	PFSK-1	brain:	n/a
18	chr19:45147316-45147366	BJ	skin:	n/a
19	chr19:45147440-45147490	NH-A	brain:	n/a
20	chr19:45147440-45147490	SK-N-MC	brain:	n/a
21	chr19:45147316-45147366	HepG2	liver:	n/a
22	chr19:45147440-45147490	SKMC	muscle:	n/a
23	chr19:45147316-45147366	HCF	heart:	n/a
24	chr19:45147440-45147490	HAEpiC	amniotic membrane:	n/a
25	chr19:45147316-45147366	HAEpiC	amniotic membrane:	n/a
26	chr19:45147715-45147765	AG09319	gingival:	n/a
27	chr19:45147316-45147366	GM06990	blood:	n/a
28	chr19:45147316-45147366	ovcar-3	ovarian:	n/a
29	chr19:45147440-45147490	AoSMC	blood vessel:	n/a
30	chr19:45147715-45147765	NH-A	brain:	n/a
31	chr19:45147316-45147366	Jurkat	blood:	n/a
32	chr19:45147715-45147765	RPTEC	kidney:	n/a
33	chr19:45147440-45147490	ECC-1	luminal epithelium:	n/a
34	chr19:45147715-45147765	H1-hESC	embryonic stem cell:	embryo
35	chr19:45147440-45147490	LNCaP	prostate:	n/a
36	chr19:45147715-45147765	Hepatocyte	liver:	n/a
37	chr19:45147440-45147490	CMK	blood:	n/a
38	chr19:45147715-45147765	HUVEC	blood vessel:	n/a
39	chr19:45147316-45147366	AG10803	skin:	n/a
40	chr19:45147316-45147366	GM12878	blood:	n/a
41	chr19:45147715-45147765	SAEC	small airway:	n/a
42	chr19:45147440-45147490	SK-N-SH_RA	brain:	n/a
43	chr19:45147316-45147366	H1-hESC	embryonic stem cell:	embryo
44	chr19:45147440-45147490	GM06990	blood:	n/a
45	chr19:45147715-45147765	T-47D	breast:	n/a
46	chr19:45147316-45147366	HUVEC	blood vessel:	n/a
47	chr19:45147715-45147765	BE2_C	brain:	n/a
48	chr19:45147316-45147366	LNCaP	prostate:	n/a
49	chr19:45147316-45147366	IMR90	lung:	fetal
50	chr19:45147440-45147490	HRE	kidney:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:44258125..44259814-chr19:45145810..45147652,2	MCF-7	breast:
2	chr19:45149403..45152148-chr19:45154474..45156366,2	K562	blood:
3	chr19:45147094..45148808-chr19:45149467..45152344,2	MCF-7	breast:
4	chr14:81686687..81687304-chr19:45147100..45147918,2	Hela-S3	cervix:
5	chr19:6110486..6111008-chr19:45146836..45147494,2	HCT-116	colon:
6	chr19:45148126..45150959-chr19:45153045..45156023,2	K562	blood:
7	chr19:45147274..45147946-chr3:101568067..101568848,2	Hela-S3	cervix:
8	chr19:45149710..45152694-chr19:45240654..45242344,2	MCF-7	breast:
9	chr19:45146195..45148606-chr19:45175248..45176784,2	MCF-7	breast:

No data

Variant related genes	Relation type
PVR	TF binding region
PVR	CpG island
ENSG00000186567	chromatin interactions
ENSG00000073008	chromatin interactions
ENSG00000144802	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000087903	chromatin interactions
ENSG00000105771	chromatin interactions

Extended variants
information (count: 130 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:130 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs430341	chr19:45147146-45147147	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs552074006	chr19:45147237-45147238	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs369448826	chr19:45147244-45147245	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs534809961	chr19:45147280-45147281	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs567374931	chr19:45147291-45147292	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs11540084	chr19:45147340-45147341	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs112304208	chr19:45147362-45147363	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs11540085	chr19:45147396-45147397	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs80109069	chr19:45147440-45147441	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs556963270	chr19:45147498-45147499	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs72528715	chr19:45147517-45147518	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs111420496	chr19:45147518-45147519	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs34158234	chr19:45147519-45147520	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs439446	chr19:45147542-45147543	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs539469356	chr19:45147571-45147572	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs5828212	chr19:45147577-45147578	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs34957576	chr19:45147589-45147590	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs112989771	chr19:45147606-45147607	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs114507600	chr19:45147607-45147608	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs113672371	chr19:45147610-45147611	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs573497914	chr19:45147616-45147617	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs377093980	chr19:45147686-45147687	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs562146780	chr19:45147705-45147706	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs10426401	chr19:45147719-45147720	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs544311749	chr19:45147720-45147721	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs536823151	chr19:45147745-45147746	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs139223077	chr19:45147768-45147769	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs533132038	chr19:45147784-45147785	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs546631637	chr19:45147791-45147792	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs559597721	chr19:45147836-45147837	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs556747279	chr19:45147838-45147839	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs528381229	chr19:45147855-45147856	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs548328813	chr19:45147864-45147865	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs568177534	chr19:45147872-45147873	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs116753796	chr19:45147912-45147913	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs144071531	chr19:45147976-45147977	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs150985779	chr19:45147992-45147993	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs11362724	chr19:45148020-45148021	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574192982	chr19:45148021-45148022	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs398034756	chr19:45148036-45148037	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs112403827	chr19:45148039-45148040	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs539429175	chr19:45148046-45148047	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs11360299	chr19:45148054-45148055	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190775300	chr19:45148089-45148090	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs567106634	chr19:45148110-45148111	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547819052	chr19:45148118-45148119	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs555892628	chr19:45148120-45148121	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs575768284	chr19:45148121-45148122	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533976680	chr19:45148138-45148139	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs373060085	chr19:45148152-45148153	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Adrenocortical carcinoma	18281524	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:45146400-45147400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr19:45146600-45147200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
3	chr19:45146600-45147200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr19:45146600-45147200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr19:45146600-45147200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr19:45146600-45147600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
7	chr19:45146600-45147600	Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr19:45146600-45147800	Active TSS	Brain Hippocampus Middle	brain
9	chr19:45146600-45148200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr19:45146600-45148200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr19:45146600-45148200	Active TSS	Liver	Liver
12	chr19:45146600-45148200	Active TSS	Brain Cingulate Gyrus	brain
13	chr19:45146600-45148200	Active TSS	Rectal Smooth Muscle	rectum
14	chr19:45146600-45148400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr19:45146600-45148800	Active TSS	Psoas Muscle	Psoas
16	chr19:45146600-45148800	Active TSS	NH-A	brain
17	chr19:45146600-45149200	Active TSS	Osteobl	bone
18	chr19:45146800-45147200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
19	chr19:45146800-45147200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr19:45146800-45147200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr19:45146800-45147200	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr19:45146800-45147200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr19:45146800-45147200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr19:45146800-45147200	Flanking Active TSS	Primary hematopoietic stem cells	blood
25	chr19:45146800-45147200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr19:45146800-45147200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
27	chr19:45146800-45147200	Flanking Active TSS	Adipose Nuclei	Adipose
28	chr19:45146800-45147200	Flanking Active TSS	Esophagus	oesophagus
29	chr19:45146800-45147200	Flanking Active TSS	Fetal Muscle Leg	muscle
30	chr19:45146800-45147200	Flanking Active TSS	Right Ventricle	heart
31	chr19:45146800-45147200	Enhancers	Spleen	Spleen
32	chr19:45146800-45147200	Flanking Active TSS	HMEC	breast
33	chr19:45146800-45147200	Flanking Active TSS	HUVEC	blood vessel
34	chr19:45146800-45147200	Flanking Active TSS	NHLF	lung
35	chr19:45146800-45147400	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
36	chr19:45146800-45147400	Bivalent/Poised TSS	Primary T helper cells PMA-I stimulated	--
37	chr19:45146800-45147600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr19:45146800-45147600	Active TSS	Primary T helper naive cells from peripheral blood	blood
39	chr19:45146800-45147600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
40	chr19:45146800-45147600	Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr19:45146800-45147800	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
42	chr19:45146800-45147800	Active TSS	Thymus	Thymus
43	chr19:45146800-45148000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr19:45146800-45148000	Active TSS	Fetal Heart	heart
45	chr19:45146800-45148000	Active TSS	Gastric	stomach
46	chr19:45146800-45148200	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr19:45146800-45148200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
48	chr19:45146800-45148200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr19:45146800-45148200	Active TSS	H9 Cell Line	embryonic stem cell
50	chr19:45146800-45148200	Active TSS	Primary T cells from cord blood	blood

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